A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216141



Internal ID20783181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169546601..170309800hg38UCSC Ensembl
chr6:169946697..170618888hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38763200
hg19672192
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615772
Supporting Variants
Samples
Known GenesC6orf120, DLL1, ERMARD, FAM120B, FLJ38122, LINC00242, LINC00574, LOC154449, PHF10, TCTE3, WDR27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216141
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01227


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